Canonical Allele Identifier: CA833583461

Gene:

Linked Data

• dbSNP Id: rs1186988037
• MyVariant Identifiers: chr7:g.13440253G>A (hg19) ; chr7:g.13400628G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.13400628G>A , CM000669.2:g.13400628G>A	GRCh38
NC_000007.13:g.13440253G>A , CM000669.1:g.13440253G>A	GRCh37
NC_000007.12:g.13406778G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001745097.1:n.147+90305G>A